- Trials with a EudraCT protocol (17)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
17 result(s) found for: Tendinitis.
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EudraCT Number: 2010-020513-87 | Sponsor Protocol Number: Q03-09-01 | Start Date*: 2010-09-02 | |||||||||||
Sponsor Name:FIDIA | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind study on the intensity and duration of efficacy of sodium hyaluronate therapy (500-730 KDa) (HYALGAN) in the conservative treatment of Achilles tendin... | |||||||||||||
Medical condition: Achilles tendinopathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002856-32 | Sponsor Protocol Number: 7148L05 | Start Date*: 2004-11-18 | |||||||||||
Sponsor Name:ZAMBON GROUP | |||||||||||||
Full Title: Ketoprofen TDS patch Keofix in the treatment of flare-ups of non articular rheumatisms. A double blind, double dummy study vs oral ketoprofen retard 200 mg capsules | |||||||||||||
Medical condition: non articular rheumatism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003587-36 | Sponsor Protocol Number: 684/MODREC/15 | Start Date*: 2016-04-13 | ||||||||||||||||
Sponsor Name:Directorate of Defence Rehabilitation | ||||||||||||||||||
Full Title: Chronic Tendinopathy: The Biomechanical Associations and EfFicacy of Injectable Therapy (BE FIT) Study | ||||||||||||||||||
Medical condition: Chronic degenerative Achilles and patella tendinopathy patients, with neovascularisation on USS, who have failed best practice rehabilitation including Eccentric Loading (EL), Heavy Slow Resistance... | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021869-73 | Sponsor Protocol Number: 33178 | Start Date*: 2011-01-25 | ||||||||||||||||||||||||||
Sponsor Name:OrthoCell Pty Ltd | ||||||||||||||||||||||||||||
Full Title: The value of Autologous Tenocyte Implantation in patients with chronic Achilles tendinopathy: a double-blind randomised clinical trial | ||||||||||||||||||||||||||||
Medical condition: Chronic midportion Achilles tendinopathy | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005421-40 | Sponsor Protocol Number: RCSI-1764 | Start Date*: 2016-06-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Royal College of Surgeons in Ireland | |||||||||||||||||||||||||||||||||
Full Title: The use of topical Glyceryl Trinitrate (GTN) and eccentric exercises in the treatment of mid portion Achilles Tendinopathy: a randomised placebo controlled trial | |||||||||||||||||||||||||||||||||
Medical condition: Achilles tendinopathy | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-005087-24 | Sponsor Protocol Number: Version 2 23/03/2005. | Start Date*: 2005-07-11 |
Sponsor Name:University Hospitals of Leicester NHS Trust | ||
Full Title: CIMETIDINE IN THE TREATMENT OF CALCIFIC SUPRASPINATUS TENDINITIS- A TRIAL OF CIMETIDINE 200mg B.D IN THE RESOLUTION OF CALCIFICATION IN THE SUPRASINATUS TENDON. | ||
Medical condition: CALCIFIC SUPRASPINATUS TENDINITIS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003238-29 | Sponsor Protocol Number: BRN-C-2015-03 | Start Date*: 2016-04-06 |
Sponsor Name:Fundación Sociedad Española de Médicos de Atención Primaria (SEMERGEN) | ||
Full Title: Pilot phase II clinical trial, randomized, double-blind, controlled, single-center study to evaluate the efficacy and safety of Solanum malacoxylon 9CH in patients with calcific tendinitis of shoulder | ||
Medical condition: Calcific tendinitis of shoulder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011339-11 | Sponsor Protocol Number: PRP-H1 | Start Date*: 2009-07-07 | ||||||||||||||||
Sponsor Name:daniel pacha vicente | ||||||||||||||||||
Full Title: Estudio clínico prospectivo y randomizado comparando la inyección subacromial de plasma rico en plaquetas o de betametasona y bupivacaina en la tendinosis del manguito rotador del hombro. | ||||||||||||||||||
Medical condition: tendinitis cronica o tendinosis del manguito rotador del hombro | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001262-28 | Sponsor Protocol Number: MSC-TENDO-2015 | Start Date*: 2017-08-21 | |||||||||||
Sponsor Name:Institut de Terapia Regenerativa Tissular S.L. (ITRT) | |||||||||||||
Full Title: Treatment of Refractory Patellar Tendinopathy with MSV *. Comparative study with P-PRP *MSV are bone marrow autologous mesenchymal stem cells, selected and cultured under Good manufacturing Practic... | |||||||||||||
Medical condition: Patients diagnosed with patellar tendinopathy with a minimum of 4 months evolution and have presented two acute episodes, refractory to standard treatments present a gap equal or greater than 3 mm ... | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001709-85 | Sponsor Protocol Number: 10.05.7 | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:South Eastern Health and Social Care Trust | |||||||||||||
Full Title: Treatment of Shoulder Capsulitis by single or Multiple Corticosteroid Injections | |||||||||||||
Medical condition: Capsulitis of the Shoulder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005030-11 | Sponsor Protocol Number: 12I-BMT08 | Start Date*: 2013-02-11 | ||||||||||||||||||||||||||
Sponsor Name:IBSA INSTITUT BIOCHIMIQUE SA | ||||||||||||||||||||||||||||
Full Title: Multicentre, randomized, double-blind, placebo-controlled clinical trial to evaluate the short-term efficacy and safety of two different treatment regimens of Betamethasone valerate 2.25 mg medicat... | ||||||||||||||||||||||||||||
Medical condition: Chronic Lateral Elbow Tendinopathy and Chronic Midportion (or non-insertional) Achilles Tendinopathy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002343-34 | Sponsor Protocol Number: KALK1183 | Start Date*: 2015-10-15 |
Sponsor Name:Martina Hansens Hospital | ||
Full Title: Treatment of calcific tendinitis of the Rotator Cuff A randomized, double blinded, sham controlled, international, multicenter study | ||
Medical condition: Calcific tendinitis of the shoulder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004117-40 | Sponsor Protocol Number: Q03.13.01 | Start Date*: 2013-12-19 |
Sponsor Name:Fidia Farmaceutici SpA | ||
Full Title: Randomized, controlled, double-blinded clinical trial, with open-label extension on the efficacy of ultrasound guided injection of hyaluronic acid (500-730 KDa) (HYALGAN®) versus saline solution in... | ||
Medical condition: Achilles tendinopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024641-71 | Sponsor Protocol Number: 071(D)SC10102 | Start Date*: 2011-05-12 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: A randomized, multicenter, double-blind study assessing the efficacy and safety of two topical 10% naproxen gel formulations in the treatment of benign soft-tissue injuries. | |||||||||||||
Medical condition: Benign soft-tissue injuries. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001056-19 | Sponsor Protocol Number: HUPA-EC-02-2012 | Start Date*: 2013-12-01 | |||||||||||
Sponsor Name:FUNDACIÓN PARA LA INVESTIGACIÓN BIOMÉDICA DEL HOSPITAL UNIVERSITARIO PRÍNCIPE DE ASTURIAS | |||||||||||||
Full Title: ROLE OF BIOLOGICAL THERAPY IN ROTATOR CUFF TENDINOPATHY. EFFECTIVENESS OF PLASMA RICH IN GROWTH FACTOR (PRGF-ENDORET)REGARDING TO FUNCTIONAL CAPACITY AND PAIN COMPARED WITH THE CONVENTIONAL TREATME... | |||||||||||||
Medical condition: ROTATOR CUFF TENDINOPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004734-15 | Sponsor Protocol Number: EBio | Start Date*: 2019-06-03 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: EBIO – Enthesitis biopsy study | |||||||||||||
Medical condition: Psoriatic arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001863-31 | Sponsor Protocol Number: LR-07 | Start Date*: 2009-03-12 | ||||||||||||||||
Sponsor Name:Hospital Universitario de Bellvitge | ||||||||||||||||||
Full Title: Estudio Comparativo de la Eficacia de Pautas “Cortas” y “Largas” de la Combinación Rifampicina-Levofloxacino en la Infección Estafilocócica Postquirúrgica Precoz y Hematógena de Prótesis Articular ... | ||||||||||||||||||
Medical condition: El tratamiento de elección de la infección precoz postquirúrgica y hematógena de prótesis articular con implante estable es el desbridamiento precoz con retención del material y un tratamiento anti... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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